Gene Expression Patterns Associated with Survival in Glioblastoma

Author:

Morrison Christopher1ORCID,Weterings Eric1,Gravbrot Nicholas2ORCID,Hammer Michael23ORCID,Weinand Martin4,Sanan Abhay5,Pandey Ritu6,Mahadevan Daruka7,Stea Baldassarre1ORCID

Affiliation:

1. Department of Radiation Oncology, University of Arizona, Tucson, AZ 85719, USA

2. College of Medicine, University of Arizona, Tucson Campus, Tucson, AZ 85724, USA

3. Department of Neurology, University of Arizona Genetics Core, Tucson, AZ 85724, USA

4. Department of Neurosurgery, University of Arizona, Tucson, AZ 85724, USA

5. Center for Neurosciences, Tucson, AZ 85719, USA

6. Department of Cellular and Molecular Medicine, University of Arizona Cancer Center Bioinformatics Shared Resource, and College of Medicine, University of Arizona, Tucson, AZ 85724, USA

7. Mays Cancer Center, University of Texas Health, San Antonio, TX 78229, USA

Abstract

The aim of this study was to investigate gene expression alterations associated with overall survival (OS) in glioblastoma (GBM). Using the Nanostring nCounter platform, we identified four genes (COL1A2, IGFBP3, NGFR, and WIF1) that achieved statistical significance when comparing GBM with non-neoplastic brain tissue. The four genes were included in a multivariate Cox Proportional Hazard model, along with age, extent of resection, and O6-methylguanine-DNA methyltransferase (MGMT) promotor methylation, to create a unique glioblastoma prognostic index (GPI). The GPI score inversely correlated with survival: patient with a high GPI had a median OS of 7.5 months (18-month OS = 9.7%) whereas patients with a low GPI had a median OS of 20.1 months (18-month OS = 54.5%; log rank p-value = 0.004). The GPI score was then validated in 188 GBM patients from The Cancer Genome Atlas (TCGA) from a national data base; similarly, patients with a high GPI had a median OS of 10.5 months (18-month OS = 12.4%) versus 16.9 months (18-month OS = 41.5%) for low GPI (log rank p-value = 0.0003). We conclude that this novel mRNA-based prognostic index could be useful in classifying GBM patients into risk groups and refine prognosis estimates to better inform treatment decisions or stratification into clinical trials.

Funder

Robert Sharpe Foundation

Community Foundation for Southern Arizona

University of Arizona Cancer Center

Publisher

MDPI AG

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